| scholarly article | Q13442814 |
| P50 | author | Lilia Perfeito | Q60167859 |
| Isabel Gordo | Q41582649 | ||
| Ana Sousa | Q42113509 | ||
| P2860 | cites work | Molecular Evolution Over the Mutational Landscape | Q22064602 |
| High Frequency of Cryptic Deleterious Mutations in Caenorhabditis elegans | Q22065551 | ||
| Long-Term Experimental Evolution in Escherichia coli. I. Adaptation and Divergence During 2,000 Generations | Q22066139 | ||
| Fitness effects of advantageous mutations in evolving Escherichia coli populations | Q22066182 | ||
| Fitness and its role in evolutionary genetics | Q22122004 | ||
| The distribution of fitness effects of new mutations | Q22122013 | ||
| Distribution of fitness effects among beneficial mutations before selection in experimental populations of bacteria | Q22122042 | ||
| Construction of Escherichia coli K-12 in-frame, single-gene knockout mutants: the Keio collection | Q22122301 | ||
| Lateral gene transfer and the nature of bacterial innovation | Q22122396 | ||
| A constant rate of spontaneous mutation in DNA-based microbes | Q28271032 | ||
| Pervasive Cryptic Epistasis in Molecular Evolution | Q28475868 | ||
| Pervasive sign epistasis between conjugative plasmids and drug-resistance chromosomal mutations | Q28476356 | ||
| A framework for evolutionary systems biology | Q28754894 | ||
| Mechanistic approaches to the study of evolution: the functional synthesis | Q28757580 | ||
| Escherichia coli K-12 undergoes adaptive evolution to achieve in silico predicted optimal growth | Q29397612 | ||
| Darwinian evolution can follow only very few mutational paths to fitter proteins | Q29616042 | ||
| Global transposon mutagenesis and a minimal Mycoplasma genome | Q29617096 | ||
| Mutation accumulation in Tetrahymena | Q30497610 | ||
| Direct estimation of the mitochondrial DNA mutation rate in Drosophila melanogaster | Q33361751 | ||
| Periodic selection in Escherichia coli | Q33711273 | ||
| Phenotypic landscape of a bacterial cell | Q33780274 | ||
| Beneficial mutations and the dynamics of adaptation in asexual populations. | Q33856627 | ||
| Forces that influence the evolution of codon bias | Q33856645 | ||
| Escherichia coli rpoB mutants have increased evolvability in proportion to their fitness defects | Q33860371 | ||
| Nonlinear fitness landscape of a molecular pathway | Q33981298 | ||
| Frequent beneficial mutations during single-colony serial transfer of Streptococcus pneumoniae. | Q34005325 | ||
| The speed of evolution and maintenance of variation in asexual populations | Q34330675 | ||
| Genetic bottlenecks reduce population variation in an experimental RNA virus population | Q34348294 | ||
| Missense meanderings in sequence space: a biophysical view of protein evolution | Q34439602 | ||
| Diminishing Returns from Mutation Supply Rate in Asexual Populations | Q56920120 | ||
| Rate of deleterious mutation and the distribution of its effects on fitness in vesicular stomatitis virus | Q57052385 | ||
| The solitary wave of asexual evolution | Q34470274 | ||
| The noisy edge of traveling waves | Q34549815 | ||
| Spontaneous mutations in diploid Saccharomyces cerevisiae: more beneficial than expected | Q34569445 | ||
| Direct estimation of per nucleotide and genomic deleterious mutation rates in Drosophila | Q34597710 | ||
| Mutation accumulation in populations of varying size: the distribution of mutational effects for fitness correlates in Caenorhabditis elegans | Q34643894 | ||
| Adaptive mutations in bacteria: high rate and small effects | Q34661718 | ||
| A biophysical protein folding model accounts for most mutational fitness effects in viruses | Q35049281 | ||
| Dynamics of insertion sequence elements during experimental evolution of bacteria | Q35811200 | ||
| Resistance of virus to extinction on bottleneck passages: study of a decaying and fluctuating pattern of fitness loss | Q35978399 | ||
| Genomic mutation rates for lifetime reproductive output and lifespan in Caenorhabditis elegans | Q36105992 | ||
| Theories of adaptation: what they do and don't say. | Q36120420 | ||
| Genomic evolution during a 10,000-generation experiment with bacteria | Q36451882 | ||
| The distribution of beneficial and fixed mutation fitness effects close to an optimum | Q36724374 | ||
| Whole-genome mutational biases in bacteria | Q36976728 | ||
| Rate and effects of spontaneous mutations that affect fitness in mutator Escherichia coli | Q37716243 | ||
| Mutations of intermediate effect are responsible for adaptation in evolving Pseudomonas fluorescens populations | Q38786690 | ||
| Frequency-dependent selection in bacterial populations | Q39471728 | ||
| Target site selection in transposition | Q41550231 | ||
| On measuring selection in experimental evolution. | Q42076622 | ||
| The distribution of fitness effects of new beneficial mutations in Pseudomonas fluorescens | Q42585639 | ||
| Fitness declines in Tobacco etch virus upon serial bottleneck transfers | Q42737923 | ||
| Update on the Keio collection of Escherichia coli single-gene deletion mutants | Q42912234 | ||
| Synergistic fitness interactions and a high frequency of beneficial changes among mutations accumulated under relaxed selection in Saccharomyces cerevisiae | Q43092006 | ||
| Compensatory adaptation to the deleterious effect of antibiotic resistance in Salmonella typhimurium | Q44666207 | ||
| Intercellular nanotubes mediate bacterial communication. | Q45941890 | ||
| Comparative genome sequencing of Escherichia coli allows observation of bacterial evolution on a laboratory timescale | Q46069507 | ||
| Evolution of a bacteria/plasmid association | Q46676230 | ||
| Mutational robustness of ribosomal protein genes | Q50045244 | ||
| Genomic buffering mitigates the effects of deleterious mutations in bacteria | Q50085780 | ||
| An equivalence principle for the incorporation of favorable mutations in asexual populations. | Q50736355 | ||
| Estimate of the genomic mutation rate deleterious to overall fitness in E. coli. | Q51030744 | ||
| The fitness effect of mutations across environments: a survey in light of fitness landscape models. | Q51714236 | ||
| Distributed robustness versus redundancy as causes of mutational robustness. | Q52654713 | ||
| High direct estimate of the mutation rate in the mitochondrial genome of Caenorhabditis elegans. | Q52925865 | ||
| Fitness effects of fixed beneficial mutations in microbial populations. | Q54541810 | ||
| Reducing antibiotic resistance. | Q54588726 | ||
| The evolution of functionally novel proteins after gene duplication. | Q55065818 | ||
| P433 | issue | 1-2 | |
| P304 | page(s) | 20-35 | |
| P577 | publication date | 2011-01-01 | |
| P1433 | published in | Journal of Molecular Microbiology and Biotechnology | Q15767392 |
| P1476 | title | Fitness effects of mutations in bacteria | |
| P478 | volume | 21 |
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